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   <subfield code="a">A new high-pressure and high-temperature polymorph of FeS</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Hiroaki Ohfuji, Nagayoshi Sata, Hisao Kobayashi, Yasuo Ohishi, Kei Hirose, Tetsuo Irifune]</subfield>
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   <subfield code="a">A new polymorph of FeS has been observed at pressures above 30GPa at 1,300K by in situ synchrotron X-ray diffraction measurements in a laser-heated diamond anvil cell. It is stable up to, at least, 170GPa at 1,300K. The new phase (here called FeS VI) has an orthorhombic unit cell with lattice parameters a=4.8322 (17)Å, b=3.0321 (6)Å, and c=5.0209 (8)Å at 85GPa and 300K. Its topological framework is based on the NiAs-type structure as is the case for the other reported polymorphs (FeS I-V). The unit cell of FeS VI is, however, more distorted (contracted) along the [010] direction of the original NiAs-type cell. For example, the c/b axial ratio is ∼1.66 at 85GPa and 300K, which is considerably smaller than that of orthorhombic FeS II (∼1.72) and NiAs-type hexagonal FeS V (=√3≈1.73). The phase boundary between FeS IV and VI is expected to be located around 30GPa at 1,300K. The phase transition is accompanied by gradual and continuous changes in volume and axial ratios and may be second order. At room temperature, FeS VI becomes stable over FeS III at pressures above 36GPa. It is, therefore, suggested that the phase boundary of FeS III-VI and/or FeS IV-VI has negative pressure dependence.</subfield>
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